I‘ve learned that it’s important to be selective and rely on only certain websites for factual information about your disease(s), and you must also be discriminatory with medications and supplements.
Even if you don't know someone in your city with your particular disease, you are not alone in your struggles. Reach out and find someone online to help support you through this.
I learned of this organization during the pandemic. Their emails contain important resources for those of us with poor immune systems.
The Lupus Foundation of America will keep you updated with the latest research, resources, and clinical trials for treatments. Also, check out Lupus Corner: https://lupuscorner.com
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